Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 63992생성일: 2026년 10월 24일
1-Pyrrolidinecarboxylic acid, 2-oxo-, 1,1-dimethylethyl ester → tert-butyl N-[4-(3-fluorophenyl)-4-oxobutyl]carbamate
https://huagongshe.com/ko/reaction/63992
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Pyrrolidinecarboxylic acid, 2-oxo-, 1,1-dimethylethyl ester | HCID 379000 | — |
| 반응물 | HCID 178505773 | HCID 178505773 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | tert-butyl N-[4-(3-fluorophenyl)-4-oxobutyl]carbamate | HCID 67330612 | — |
반응 단계
In a round-bottomed flask was charged tert-butyl 2-oxopyrrolidine-1-carboxylate (2.2 g, 11.9 mmol) and THF (25 mL). The mixture was cooled down to −78° C. first, followed by slow addition of (3-fluorophenyl)magnesium bromide (17.8 mL, 17.8 mmol, 1.0 M solution in THF) over 15 minutes. The mixture was stirred for 3 hours, during which time the bath temperature rose from −78° C. to −10° C. The reaction was quenched by drop-wise addition of 1N HCl (2 mL) and warmed up to ambient temperature, followed by addition of EtOAc and water. After separating the organic layer, the aqueous layer was extracted with EtOAc three times. The combined organic layers was dried over Na2SO4 and concentrated to yield the product as a clear oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09447104B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-0e0d6802bbec4410b6ba92c729e66ce8 |
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| 출처 메모 | uspto-grants-2016_09 |
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